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Tums Chewy Delights calcium carbonate 1177 mg Bar, Chewable, 32-count — NDC 00135-0569-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Tums Chewy Delights calcium carbonate 1177 mg Bar, Chewable, 32-count — NDC 0135-0569-01 (Billing 00135-0569-01)

by Haleon US Holdings LLC · 32 BAR, CHEWABLE in 1 BAG

This is a package of 32 bars of Tums Chewy Delights calcium carbonate 1177 mg Bar, Chewable from Haleon US Holdings LLC, marketed since Aug 2014 and currently FDA-listed. It is this product's only package size.

NDC 00135-0569-01
🏷️ FDA NDC (as labeled) 0135-0569-01 billing pads the labeler segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 0135-0569-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
0135 labeler · 0569 product · 01 package
Package marketed since
Aug 15, 2014
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Billing quantity
32 EA per package
Barcode (UPC-A, from the NDC)
3 0135056901 9
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Calcium Carbonate (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0573-2026
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0561-2026
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0578-2026
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0568-2026
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0579-2026
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0560-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0135-0569-01
Product NDC 0135-0569
11-digit billing NDC 00135056901
NCPDP billing unit EA — each (per item)
RxCUI 1432465, 1653049
UNII H0G9379FGK
Application # M001
SPL Set ID 189850d0-6f06-45bd-bd7e-9063ee580d0b
Established class (EPC) Blood Coagulation Factor; Cations; Phosphate Binder
Mechanism of action Phosphate Chelating Activity
Physiologic effect Increased Coagulation Factor Activity
Chemical class Calcium; Divalent
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2014-08-15
Route ORAL
Dosage form BAR, CHEWABLE
Substance CALCIUM CARBONATE

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GPI-14 48300010000550
GPI class Tums Chewy Delights
Quick answers
  • GPI-14 (Medi-Span): 48300010000550
  • RxCUI (RxNorm): 1432465
Why two NDCs? The FDA registers this code as 0135-0569-01 — a 4-4-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the labeler segment → 00135-0569-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Calcium compounds class.

Drug family (ATC) Calcium compounds, Calcium
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

📖 What it is MedlinePlus · NLM

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • Most often it's an antacid. It relieves heartburn, acid indigestion, sour stomach and upset stomach tied to those symptoms. A few supplement products have other uses, like bone sup...
  • What is calcium carbonate usually used for?
  • You chew it when symptoms come on. Many labels say to chew or crush the tablets completely and not swallow them whole. The number of tablets varies by product, so read your label o...
  • Many labels say not to use the maximum dose for more than 2 weeks unless a doctor is supervising you. If your symptoms last longer than 2 weeks, check in with your doctor.
📖 Read our full Calcium Carbonate guide →
4
Nutrient depletion considerations

Calcium Carbonate may be associated with lower levels of 4 nutrients — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Calcium Carbonate nutrient depletion report →
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
00135-0569-01 You're viewing this Main listing 32 BAR, CHEWABLE in 1 BAG 2014-08-15 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Tums Chewy Delights 1177 mg 00135-0560-01 Haleon 32 bars — — FDA listed —
Tums Chewy Delights 1177 mg 00135-0561-01 Haleon 32 bars — — FDA listed —
Tums Chewy Delights 1177 mgthis 00135-0569-01 Haleon 32 bars — — FDA listed —
Antacid Soft Chew 1177 mg 00363-1081-32 Walgreen 32 tablets — — FDA listed —
Cherry Antacid Relief Chew 1177 mg 11822-0040-01 Rite 32 tablets — — FDA listed —
Kroger Cherry Antacid Soft Chew 1177 mg 30142-0267-32 Kroger 32 tablets — — FDA listed —
Cherry Antacid Soft Chew 1177 mg 37808-0058-36 HEB 36 tablets — — FDA listed —
Cherry Antacid Soft Chews 1177 mg 41250-0109-36 Meijer 36 tablets — — FDA listed —
cherry antacid soft chew 1177 mg 41520-0031-36 American 36 tablets — — FDA listed —
HyVee Ultra Strength Antacid Soft Chews Cherry 1177 mg 42507-0921-32 Hy-Vee 32 tablets — — FDA listed —
Cherry Antacid Soft Chews 1177 mg 49035-0046-32 Walmart 32 tablets — — FDA listed —
Good Sense Antacid Soft Chew 1177 mg 50804-0027-36 Geiss, 36 tablets — — FDA listed —
Exchange Select Antacid Soft Chews Cherry Flavor 1177 mg 55301-0591-32 Army 32 tablets — — FDA listed —
Family Wellness Antacid Relief Chews 1177 mg 55319-0049-32 Family 32 tablets — — FDA listed —
Orange Antacid Soft Chew 1177 mg 69842-0363-36 CVS 36 tablets — — FDA listed —
Cherry Antacid Soft Chews 1177 mg 69842-0368-36 CVS 36 tablets — — FDA listed —
Amazon Basics Cherry Antacid SC 1177 mg 72288-0240-32 Amazon 32 tablets — — FDA listed —
TopCare Cherry Antacid Soft Chews 1177 mg 76162-0404-32 TopCo 32 tablets — — FDA listed —
Caring Mill Antacid 1177 mg 81522-0360-32 FSA 32 tablets — — FDA listed —
MGC Health Antacid Soft Chews Cherry Flavor 1177 mg 83173-0130-32 Medical 32 tablets — — FDA listed —
QC Ultra Strength Antacid Soft Chews, Cherry 1177 mg 83324-0263-32 Chain 32 tablets — — FDA listed —
MGC Health Antacid Soft Chews Cherry Flavor 1177 mg 83698-0130-32 Xiamen 32 tablets — — FDA listed —
QC Ultra Strength Antacid Soft Chews, Cherry 1177 mg 83698-0263-32 Xiamen 32 tablets — — FDA listed —
Caring Mill Antacid 1177 mg 83698-0360-32 Xiamen 32 tablets — — FDA listed —
Exchange Select Antacid Soft Chews Cherry Flavor 1177 mg 83698-0591-32 Xiamen 32 tablets — — FDA listed —
HyVee Ultra Strength Antacid Soft Chews Cherry 1177 mg 83698-0921-32 Xiamen 32 tablets — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2014
On the market since
Aug 2014
📍
2026
Currently FDA-listed
12 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

What it looks like

Color white / pink / orange
ShapeRectangle
Size21 mm
ScoringNot scored
FlavorOrange
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII LMI26O6933
    Alumina is a white powder form of aluminum oxide. It's used as a filler to add bulk to tablets and capsules, and sometimes as a thickening or anti-caking agent in powdered formulations.
  • UNII 9G5L16BK6N
    A thick, sweet liquid made from corn starch. It acts as a sweetener, thickener, and binder in medicines, helping create the right texture and taste while holding ingredients together.
  • UNII 917J3173FT
    Cow milk is a natural liquid from dairy cattle containing proteins, fats, and lactose. It's used in medicines as a source of lactose (a filler and sweetener) and milk proteins that can help bind ingredients together in tablets and capsules.
  • UNII H77VEI93A8
    A synthetic yellow dye used to color medications. It helps identify the drug and make it visually distinctive, with no effect on how the medicine works.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII JY81OXM1OM
    A plant-based oil from coconut that has been chemically treated to solidify it. It acts as a binder and filler to help hold tablet ingredients together and give the pill its shape and firmness.
  • UNII 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
  • UNII C151H8M554
    A natural sugar derived from sugar cane or sugar beets. It's used as a sweetener, filler, and binder to improve taste, add bulk, and help hold tablet or capsule ingredients together.

10 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statescorn starch, corn syrup, corn syrup solids, FD&C blue #1, flavors, glycerin, gum arabic, hydrogenated coconut oil, non-fat dairy milk, potassium sorbate, propylene glycol, soy lecithin, sucrose corn starch, corn syrup, corn syrup solids, FD&C red #40 lake, flavors, glycerin, hydrogenated coconut oil, non-fat dairy milk, propylene glycol, soy lecithin, sucrose corn starch, corn syrup, corn syrup solids, FD&C yellow #6 lake, flavors, glycerin, hydrogenated coconut oil, modified food starch, non-fat dairy milk, propylene glycol, soy lecithin, sucrose

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerHaleon US Holdings LLC
FDA applicationM001 (OTC MONOGRAPH DRUG)
Labeler code00135
First marketedAug 2014
Product typeHuman Otc Drug
Portfolio405 products on file

More NDCs from Haleon US Holdings LLC labeler code 00135

The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Ask a Doctor or Pharmacist Before Use If 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Uses Relieves: heartburn sour stomach acid indigestion upset stomach associated with these symptoms

⏱️ Dosage and Administration 41 words ▾

Directions adults and children 12 years of age and over: chew and swallow 2-3 chews as symptoms occur, or as directed by a doctor do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

⚠️ Warnings 75 words ▾

Warnings Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs. When using this product do not take more than 6 chews in 24 hours if pregnant, do not take more than 4 chews in 24 hours do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor Keep out of reach of children.

🧪 Active Ingredient 10 words ▾

Active ingredient (in each chew) Calcium carbonate USP 1177 mg

🧪 Inactive Ingredients 90 words ▾

Inactive ingredients (Smooth Peppermint) corn starch, corn syrup, corn syrup solids, FD&C blue #1, flavors, glycerin, gum arabic, hydrogenated coconut oil, non-fat dairy milk, potassium sorbate, propylene glycol, soy lecithin, sucrose

Inactive ingredients (Very Cherry) corn starch, corn syrup, corn syrup solids, FD&C red #40 lake, flavors, glycerin, hydrogenated coconut oil, non-fat dairy milk, propylene glycol, soy lecithin, sucrose

Inactive ingredients (Orange Rush) corn starch, corn syrup, corn syrup solids, FD&C yellow #6 lake, flavors, glycerin, hydrogenated coconut oil, modified food starch, non-fat dairy milk, propylene glycol, soy lecithin, sucrose

🎯 Purpose 2 words ▾

Purpose Antacid

📄 Ask a Doctor or Pharmacist Before Use If 22 words ▾

Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.

📄 When Using This Product 46 words ▾

When using this product do not take more than 6 chews in 24 hours if pregnant, do not take more than 4 chews in 24 hours do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Questions or Comments 5 words ▾

Questions or Comments? 1-800-897-7535 weekdays

📄 Package Label / Principal Display Panel ~1 min read ▾

Principal Display Panel NDC 0135-0561-01 TUMS ® CALCIUM CARBONATE ANTACID Chewy Delights ® Smooth Peppermint ULTRA STRENGTH GOES TO WORK IN SECONDS! 32 SOFT CHEWS INDIVIDUALLY WRAPPED FAST & TASTY HEARTBURN RELIEF DAIRY Tamper Evident: Do not use if packaging is torn or damaged. Distributed By: GlaxoSmithKline Consumer Healthcare, L.P.

Moon Township, PA 15108 TUMS and logo device are trademarks of the GSK group of companies. ©2014 GSK group of companies. All Rights Reserved 103608XA Tums Chewy Delights Smooth Peppermint 32 count card

Principal Display Panel NDC 0135-0560-01 TUMS ® CALCIUM CARBONATE ANTACID Chewy Delights ® Very Cherry™ ULTRA STRENGTH GOES TO WORK IN SECONDS! 32 SOFT CHEWS INDIVIDUALLY WRAPPED FAST & TASTY HEARTBURN RELIEF DAIRY Tamper Evident: Do not use if packaging is torn or damaged. Distributed By: GlaxoSmithKline Consumer Healthcare, L.P.

Moon Township, PA 15108 TUMS and logo device are trademarks of the GSK group of companies. ©2014 GSK group of companies. All Rights Reserved 103614XA Tums Chewy Delights Very Cherry 32 count card

Principal Display Panel NDC 0135-0569-01 TUMS ® CALCIUM CARBONATE ANTACID Chewy Delights ® Orange Rush™ ULTRA STRENGTH GOES TO WORK IN SECONDS! 32 SOFT CHEWS INDIVIDUALLY WRAPPED FAST & TASTY HEARTBURN RELIEF Tamper Evident: Do not use if packaging is torn or damaged. Distributed By: GlaxoSmithKline Consumer Healthcare, L.P.

Moon Township, PA 15108 TUMS and logo device are trademarks of the GSK group of companies. 103438XA Tums Chewy Delights Orange Rush 32 card

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Haleon US Holdings LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Haleon US Holdings LLC is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 00135-0568-04 · Haleon 00135-0572-02 · Haleon →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.